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Completed

NCT Number: NCT06016595

Chronic Prostatitis/Chronic Pelvic Pain Syndrome Patients

Chronic prostatitis/chronic pelvic pain syndrome (CPPS) is a common health problem among men and can cause severe quality of life. The pathophysiology of CPPS is still poorly understood and effective treatments are a challenging issue. This study aims to investigate the possible relationship between the presence of microorganisms in the prostatic fluid and symptom severity by presenting a retrospective analysis based on data from CPPS patients.

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Key information

Conditions

Chronic Prostatitis With Chronic Pelvic Pain Syndrome Genital Diseases Genital Diseases, Male Male Urogenital Diseases Prostatic Diseases Prostatitis Urogenital Diseases

Age range

20 year–60 year

Sex eligibility

Male

Study type

Observational

Primary location

Hisar Intercontinental Hospital

Istanbul, 34768, Turkey (Türkiye)

About this study

This study is based on data from 112 CPPS patients aged 20-60 years. Various variables such as demographic information of the patients, International Prostate Symptom Score (I-PSS), which evaluates CPPS symptoms, inflammatory and non-inflammatory symptoms of CPPS, baseline scores of the International Index of Erectile Function (IIEF), which evaluates erectile function, and the presence of microorganisms in the prostate fluid were analyzed retrospectively.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients who were diagnosed with chronic prostatitis/chronic pelvic pain syndrome and whose prostate fluid was taken with prostate massage and androflor testis were studied were included.

Exclusion criteria

  • acute and/or chronic bacterial prostatitis, active history of genitourinary cancer, history of recent prostate surgery the diagnosis of neurological diseases affecting the bladder was determined

Treatment and study plan

Chronic prostatitis/chronic pelvic pain syndrome

Diagnostic Test

Chronic prostatitis/chronic pelvic pain syndrome UPOINT

Primary outcomes

  1. Correlation between androflor pcr positive patients and uopint and nih-cpsi

    Time frame: 2 years

    Those with positive and negative Androflor PCR test will be evaluated. testicular torsion

Sponsors and collaborators

Lead sponsor

Hisar Intercontinental Hospital

Other

Registry information

Official study title

Retrospective Data Analysis in Chronic Prostatitis/Chronic Pelvic Pain Syndrome Patients: Evaluation of the Relationship Between Presence of Microorganism and Severity of Symptom

Important dates

Study start
2020
Primary completion
2022
Study completion
2023
First posted
Aug 29, 2023
Registry last updated
Aug 29, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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